Fastbreak: a tool for analysis and visualization of structural variations in genomic data

Genomic studies are now being undertaken on thousands of samples requiring new computational tools that can rapidly analyze data to identify clinically important features. Inferring structural variations in cancer genomes from mate-paired reads is a combinatorially difficult problem. We introduce Fa...

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Detalhes bibliográficos
Main Authors: Bressler, Ryan, Lin, Jake, Eakin, Andrea, Robinson, Thomas, Kreisberg, Richard, Rovira, Hector, Knijnenburg, Theo, Boyle, John, Shmulevich, Ilya
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3605143/
https://ncbi.nlm.nih.gov/pubmed/23046488
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1687-4153-2012-15
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